Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders.
January 18, 2023
Complete requisition forms, assemble kits for upcoming research visits, transport laboratory samples, and ensure samples are processed and shipped according to study specific guidelines, while tracking and maintaining research supplies.
February 01, 2023
Review protocol documents including abstracts, text and informed consent for relevant information.
March 29, 2023
Provide assistance upon request for the preparation of technical reports, abstracts, posters and manuscripts for submission to corporate and federal sponsors, conferences, and scientific journals.
April 10, 2023
Monitors and performs visits at satellite locations and ensures that required visits are compliant with the applicable protocol.
April 13, 2023
Act as a lead in data collection by retrieving protocol information via computer and visual chart review and by communicating directly with outlying healthcare providers to schedule and procure testing and treatment records.
April 25, 2023
Understand and adhere to the policies and procedures related to conduct of clinical trials as delineated in the Human Subject Research Manual.
April 26, 2023
Assist the Principal Investigator (PI) with protocol development, revision, and study analysis.
May 03, 2023
Following the completion of protocol required visits, the completion of source documentation occurs and data entry within the required electronic data capture system occurs in a timely manner.
May 14, 2023
